Liver disease clinical trials span a spectrum from non-alcoholic steatohepatitis (MASH/NASH) β€” where the FDA approved resmetirom in 2024 in a landmark first β€” to alcoholic hepatitis, primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC), autoimmune hepatitis, and hepatocellular carcinoma. MASH has become one of the most active areas in all of clinical medicine, driven by its rising global prevalence, progression to cirrhosis, and the now-validated principle that histological improvement is achievable.
Active MASH trials investigate THR-Ξ² agonists (resmetirom, MGL-3196), GLP-1/FGF21 combinations, FXR agonists, Pan-PPAR agonists (lanifibranor), and multi-target approaches combining metabolic and anti-fibrotic mechanisms. Hepatocellular carcinoma trials test atezolizumab plus bevacizumab combinations, lenvatinib plus pembrolizumab, and novel VEGF bispecifics. Liver fibrosis biomarkers (FIB-4, MRE-determined liver stiffness) are standard enrollment and response tools.
MASH trials typically require biopsy-confirmed NASH with fibrosis stage F1–F3 and NAS ≥4; end-stage liver disease (Child-Pugh C) is often an exclusion criterion.
Frequently Asked Questions — masld metabolic dysfunction associated steatotic liver disease Clinical Trials
How many clinical trials are currently recruiting for masld metabolic dysfunction associated steatotic liver disease?
ClinicalMetric currently tracks 3 actively recruiting clinical trials for masld metabolic dysfunction associated steatotic liver disease, sourced in real time from ClinicalTrials.gov. The total number of registered studies—including those not yet enrolling or in active follow-up—is 3. Trial availability changes daily as new studies open enrollment and existing ones reach capacity.
What trial phases are available for masld metabolic dysfunction associated steatotic liver disease?
masld metabolic dysfunction associated steatotic liver disease research spans Phase 2 (1 trial). Phase 1 studies evaluate safety and dosing in small groups, Phase 2 studies assess preliminary efficacy in 100–300 participants, and Phase 3 trials compare the new treatment against the standard of care in 300–3,000+ patients. Phase 4 post-approval studies monitor long-term outcomes in real-world populations.
How do I find out if I qualify for a masld metabolic dysfunction associated steatotic liver disease clinical trial?
Eligibility criteria for masld metabolic dysfunction associated steatotic liver disease trials vary by study and typically specify age range, disease stage or severity, prior treatment history, and specific diagnostic or laboratory parameters. Each listing on ClinicalMetric links to the full protocol on ClinicalTrials.gov, where inclusion and exclusion criteria are documented. Contact the sponsoring site's research coordinator directly to confirm your eligibility—your treating physician or specialist can also help identify the most appropriate trial based on your medical history and current treatment status.
Top Sponsors
Richmond Research Institute 1 trial
Naga P. Chalasani 1 trial
University of California, San Francisco 1 trial
Recruiting Clinical Trials
ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional.
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Last Reviewed: April 2026 ·
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